Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal T cell subset distribution (HP:0025540)

Parent Node:
Abnormal proportion of naive T cells (HP:0031396)

..Starting node
..Increased proportion of naive T cells (HP:0031398)

Term ID:

31398

Name:

Increased proportion of naive T cells

Synonym:

Elevated proportion of naive T cells; Increased proportion of naive thymus-derived, alpha-beta T cells

Definition:

An abnormally increased proportion of naive T cells relative to the total number of T cells.

Comments:

Reference:

HP:0031398

Genes and Diseases:

Child Nodes:

Sister Nodes:

Decreased proportion of naive T cells (HP:0031397)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031398	HP:0031398	Increased proportion of naive T cells	0	CL E G H
HP:0031398	HP:0410376	Increased proportion of naive CD8 T cells	1	CL E G H
HP:0031398	HP:0410375	Increased proportion of naive CD4 T cells	1	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.